IL-2-mediated upregulation of uPA and uPAR in natural killer cells

被引:11
作者
Al-Atrash, G
Shetty, S
Idell, S
Xue, YM
Kitson, RP
Halady, PKS
Goldfarb, RH
机构
[1] Univ N Texas, Hlth Sci Ctr, Dept Mol Biol & Immunol, Ft Worth, TX 76107 USA
[2] Univ N Texas, Hlth Sci Ctr, Inst Canc Res, Ft Worth, TX 76107 USA
[3] Univ Texas Hlth Ctr, Dept Med Specialties, Tyler, TX USA
关键词
NK cells; urokinase; interleukin-2; cytokines; gene regulation;
D O I
10.1006/bbrc.2002.6627
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Urokinase plasminogen activator (uPA) and its receptor uPAR play a major role in immune cell-mediated, including natural killer (NK) cell-mediated, degradation of extracellular matrices. Herein, we investigate the effects of IL-2 on NK cell uPA and uPAR. RNA and protein analyses showed upregulation of uPA and uPAR following IL-2 stimulation. Gel-shift assays and Western blots detected uPA and uPAR mRNA binding proteins (mRNABPs), previously shown to destabilize uPA and uPAR mRNA. Following IL-2 stimulation, a downregulation of uPAR mRNABP and a reciprocal induction of uPAR mRNA were noted. The increase in uPA following IL-2 stimulation appeared to be more transcriptionally regulated. These data suggest that IL-2 upregulates both uPA and uPAR in NK cells through posttranscriptional. as well as transcriptional mechanisms, partially explaining increases in NK cell invasiveness following IL-2 stimulation. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:184 / 189
页数:6
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